A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3538820



Internal ID18837101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22590297..23199681hg38UCSC Ensembl
Innerchr15:22673387..23282799hg19UCSC Ensembl
Innerchr15:20224751..20834240hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38609385
hg19609413
hg18609490
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040720
Supporting Variants
Samples
Known GenesCYFIP1, GOLGA6L1, GOLGA8DP, GOLGA8I, HERC2P2, LOC283683, MIR4509-1, MIR4509-2, MIR4509-3, NIPA1, NIPA2, TUBGCP5, WHAMMP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3538820
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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